# Avitro, LLC

- Location (FDA's records): Woodstock, IL
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: FOZ (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- App Pharmaceuticals, LLC: 1 (https://510kreport.com/company/app-pharmaceuticals)

## Its most-cited devices
- K001795: The Avitro LLC, 10 and 100 Uso Units/ML Heparin Sodium Vafd (2000), cited by 1

## Recent decisions
- K001795: The Avitro LLC, 10 and 100 Uso Units/ML Heparin Sodium Vafd (Oct 19, 2000)
- K000632: 0.9% Sodium Chloride Vasculat Access Device (Oct 19, 2000)

Source page: https://510kreport.com/company/avitro